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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laryngoscope, Rigid
510(k) Number K883296
Device Name LARYNGOSCOPE
Applicant
Lothar Scharras
C/O Rep German Industry/Trade
One Farragut Sq. S. NW
Washington,  DC  20006
Applicant Contact LOTHAR GRIESSBACH
Correspondent
Lothar Scharras
C/O Rep German Industry/Trade
One Farragut Sq. S. NW
Washington,  DC  20006
Correspondent Contact LOTHAR GRIESSBACH
Regulation Number868.5540
Classification Product Code
CCW  
Date Received08/04/1988
Decision Date 10/13/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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